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Institution

Incyte

CompanyWilmington, Delaware, United States
About: Incyte is a company organization based out in Wilmington, Delaware, United States. It is known for research contribution in the topics: Expression vector & Ruxolitinib. The organization has 1262 authors who have published 1875 publications receiving 75015 citations. The organization is also known as: Incyte Corporation & Incyte Inc..


Papers
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Journal ArticleDOI
TL;DR: A potent CCR2 antagonist 21 (INCB3344) exhibited >100-fold selectivity over other homologous chemokine receptors, a free fraction of 24% in human serum and 15% in mouse serum, and an oral bioavailability of 47% in mice, suitable as a tool compound for target validation in rodent models.

35 citations

Journal Article
Jeanne F. Loring1, J G Porter, J Seilhammer, M R Kaser, Robin L. Wesselschmidt 
TL;DR: The gene expression profiles indicate that ES cells actively suppress differentiation by transcriptional repression; cell-cell contact in embryoid bodies and retinoic acid treatment may overcome this suppression, allowing expression of Hox genes and inducing a suite of neuronal genes.
Abstract: Embryonic stem (ES) cells have the ability to differentiate into a variety of cell lineages. We are examining ES cell differentiation in vitro by using cDNA microarrays to generate a molecular phenotype for each cell type. El4 ES cells induced by retinoic acid after forming embryoid bodies differentiate almost exclusively to neurons. We obtained expression patterns for about 8500 gene sequences by comparing mRNAs from undifferentiated ES cells and their differentiated derivatives in a competitive hybridization. Our results indicate that the genes expressed by ES cells change dramatically as they differentiate (58 gene sequences up-regulated, 34 down-regulated). Most notably, totipotent ES cells expressed high levels of a repressor of Hox expression (the polycomb homolog Mphl) and a co-repressor (CTBP2). Expression of these genes was undetectable in differentiated cells; the ES cell-derived neurons expressed a different set of transcriptional regulators, as weil as markers of neurogenesis. The gene expression profiles indicate that ES cells actively suppress differentiation by transcriptional repression; cell-cell contact in embryoid bodies and retinoic acid treatment may overcome this suppression, allowing expression of Hox genes and inducing a suite of neuronal genes. Gene expression profiles will be a useful outcome measure for comparing in vitro treatments of differentiating ES cells and other stem cells. Also, knowing the molecule phenotype of transplantable cells will allow correlation of phenotype with the success of the transplant.

35 citations

Journal ArticleDOI
TL;DR: The immunosuppressive enzyme indoleamine 2, 3-dioxygenase 1 facilitates immune tolerance in cancer via T-cell suppression, and IDO1 overexpression is associated with poor tumorigenicity in mice.
Abstract: 3012Background: The immunosuppressive enzyme indoleamine 2, 3-dioxygenase 1 (IDO1) facilitates immune tolerance in cancer via T-cell suppression, and IDO1 overexpression is associated with poor sur...

35 citations

Journal ArticleDOI
16 Nov 2008-Blood
TL;DR: Treatment with INCB018424 led to resolution of the symptoms of poor appetite and early satiety, along with the reduction in splenomegaly, which improves the nutritional status of MF patients.

35 citations

Patent
Yun-Long Li1, James D. Rodgers1
18 Feb 2011
TL;DR: In this paper, the present invention relates to cyclobutane and methylcyclobutanes derivatives, as well as their salts, compositions, and methods of use, which are Janus kinase (JAK) inhibitors useful in the treatment of JAK-associated diseases including, for example, inflammatory and autoimmune disorders, and cancer and myeloproliferative disorders.
Abstract: The present invention relates to cyclobutane and methylcyclobutane derivatives, as well as their salts, compositions, and methods of use, which are Janus kinase (JAK) inhibitors useful in the treatment of JAK-associated diseases including, for example, inflammatory and autoimmune disorders, as well as cancer and myeloproliferative disorders.

35 citations


Authors

Showing all 1267 results

NameH-indexPapersCitations
Patrick O. Brown183755200985
David Botstein165468212787
Inês Barroso11330176241
Alessandro M. Vannucchi9471535482
Ana M. Valdes8433426627
Mark C. Genovese7936426945
Michael B. Eisen7117089150
Jingyue Ju6116918952
Jeanne F. Loring6017714503
James Z. Wang5722521890
Emmett V. Schmidt501509304
Günther Sperk5012410246
Robert C. Newton441117369
Magnus Pfahl44878064
William V. Williams441687278
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
20231
20225
202158
202093
201985
201882